| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13099923-13100291 | Common:5; Rare:84; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13100374-13100483 | Common:2; Rare:22 | ||||
| chr10:13100583-13100686 | Common:1; Rare:19 | ||||
| chr10:13100710-13101007 | Common:2; Rare:57 | ||||
| chr10:13161274-13161603 | Common:1; Rare:88 | ||||
| chr10:13299427-13299497 | Common:1; Rare:15 | ||||
| chr10:13299501-13299754 | Common:4; Rare:53 | ||||
| chr10:13299796-13299837 | Common:2; Rare:8 | ||||
| chr10:13299856-13300244 | Common:2; Rare:121; Clinvar:2 | ||||
| chr10:13302071-13302196 | Common:1; Rare:18 | ||||
| chr10:13302237-13302605 | Common:1; Rare:79 | ||||
| chr10:13346773-13347075 | Common:6; Rare:76 | ||||
| chr10:13347219-13347361 | Common:1; Rare:54 | ||||
| chr10:13528493-13528739 | Common:6; Rare:64 | ||||
| chr10:13528779-13529236 | Common:1; Rare:120 |